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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877105Generated: November 2, 2026

Phenacyl bromide → HCID 68512462, compound

https://huagongshe.com/reaction/1877105

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
ReactantMethyl 3-oxovalerateHCID 121699—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
SolventTolueneHCID 1140—
ProductHCID 68512462HCID 6851246258.3%

Reaction Steps

To a solution of phenacyl bromide (10 g) and methyl 3-oxopentanoate (6.5 g) in toluene (100 mL) was added dropwise 1,8-azabicyclo[5.4.0]-7-undecene (7.5 mL) over 30 min or more under ice-cooling. After the completion of the dropwise addition, the mixture was stirred for 30 min under ice-cooling and then at room temperature for 2 hr. The resulting precipitate was filtered, and washed with toluene. The obtained toluene solution was passed through silica gel, and the silica gel was washed with ethyl acetate-hexane (1:1). The collected solutions were concentrated under reduced pressure to remove ethyl acetate-hexane to give a toluene solution. To this toluene solution was added 4-toluenesulfonic acid monohydrate (1.9 g), and the mixture was stirred at 100° C. for 2 hr. The reaction mixture was washed with aqueous sodium hydrogen carbonate solution, and the aqueous layer was extracted with ethyl acetate. The organic layers were collected, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel chromatography (0% ethyl acetate/hexane to 5% ethyl acetate/hexane) to give the title compound (6.7 g, 58%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309580B2
Source datasetuspto-grants-2012_11
ORD IDord-7c496b204544445ca1653545355ead17
Source noteuspto-grants-2012_11